ATP7B Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2715066

Produktdetails

Target: ATP7B (ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 1

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses ATP7B Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human ATP7B (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: ATP7B (ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))

Andere Bezeichnung: Atp7b (ATP7B Produkte)

Synonyme: PWD Protein, WC1 Protein, WD Protein, WND Protein, Atp7a Protein, tx Protein, Hts Protein, PINA Protein, Wd Protein, ATP7B Protein, ATPase copper transporting beta Protein, ATPase, Cu++ transporting, beta polypeptide Protein, ATPase, Cu++ transporting, beta polypeptide (Wilson disease) Protein, copper-transporting ATPase 2 Protein, ATP7B Protein, Atp7b Protein, atp7b Protein, LOC592143 Protein

Hintergrund: This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD).

Molekulargewicht: 157.1 kDa

NCBI Accession: NP_000044

Pathways: Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process